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外阴黏液样脂肪肉瘤:一种罕见的外阴良性肿块样恶性肿瘤。

Myxoid Liposarcoma of the Vulva: A Rare Malignancy Mimicking Benign Vulvar Mass.

机构信息

Department of Obstetrics and Gynecology, Universitas Padjadjaran, Bandung, West Java, Indonesia.

Department of Obstetrics and Gynecology, Karisma Cimareme Hospital, Bandung, West Java, Indonesia.

出版信息

Am J Case Rep. 2022 Oct 10;23:e937575. doi: 10.12659/AJCR.937575.

Abstract

BACKGROUND Liposarcoma of the vulva is an exceptionally rare malignant tumor. Clinically, vulvar liposarcoma often mimics benign lesions, thus misdiagnosis is common. Herein, we present a case of myxoid liposarcoma of the vulva. To the best of our knowledge, this is the first case report of vulvar liposarcoma from Indonesia. CASE REPORT We present a case of a 39-year-old woman with left vulvar mass of 6 years duration that progressively increased in size. The patient reported having pressure and discomfort, especially during movement, but reported no pain. Lipoma was initially suspected. Surgical excision was performed and histopathological examination revealed a well-differentiated myxoid liposarcoma. The base and excised margins of the tumor were free of malignant cells. Post-operative course was uneventful and she was discharged in a satisfactory condition. The patient had been under regular follow-up and is currently symptom- and recurrence-free. We also review other cases of vulvar liposarcoma to further comprehend characteristics of this rare malignant tumor. CONCLUSIONS Liposarcoma of the vulva occurs very rarely, but clinicians and pathologists should always consider it as a differential diagnosis when presented with vulvar mass. Biopsy of a vulvar mass is crucial. Surgical excision remains the mainstay of treatment. Adjuvant radiotherapy may be considered in certain cases. Comprehensive follow-up for recurrences or metastasis is recommended throughout life.

摘要

背景

外阴脂肪肉瘤是一种极为罕见的恶性肿瘤。临床上,外阴脂肪肉瘤常与良性病变相混淆,因此误诊较为常见。本文报告 1 例外阴黏液样脂肪肉瘤。据我们所知,这是印度尼西亚首例外阴脂肪肉瘤的病例报告。

病例报告

我们报告了 1 例 39 岁女性,外阴左侧肿块 6 年,逐渐增大。患者自述有压迫感和不适感,尤其是在活动时,但无疼痛感。最初怀疑为脂肪瘤。行手术切除,组织病理学检查显示为分化良好的黏液样脂肪肉瘤。肿瘤的基底和切除边缘均无恶性细胞。术后恢复顺利,患者满意出院。患者定期随访,目前无任何症状和复发迹象。我们还回顾了其他外阴脂肪肉瘤病例,以进一步了解这种罕见恶性肿瘤的特征。

结论

外阴脂肪肉瘤非常罕见,但当出现外阴肿块时,临床医生和病理科医生应始终将其作为鉴别诊断。外阴肿块的活检至关重要。手术切除仍然是主要的治疗方法。某些情况下可考虑辅助放疗。建议终身进行全面随访以监测复发或转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e14/9562595/49e5d5597392/amjcaserep-23-e937575-g001.jpg

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